Canonical Allele Identifier: CA2480680312

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990925_153990936delinsCAGGGACCGCAG , CM000663.2:g.153990925_153990936delinsCAGGGACCGCAG	GRCh38
NC_000001.10:g.153963401_153963412delinsCAGGGACCGCAG , CM000663.1:g.153963401_153963412delinsCAGGGACCGCAG	GRCh37
NC_000001.9:g.152230025_152230036delinsCAGGGACCGCAG	NCBI36
NG_053102.2:g.5171_5182delinsCAGGGACCGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.5_16delinsCAGGGACCGCAG
ENST00000643794.1:c.18_29delinsCAGGGACCGCAG	ENSP00000495765.1:p.Ser6=
ENST00000651669.1:c.6+123_6+134delinsCAGGGACCGCAG MANE Select	ENSP00000499044.1:n.6+123_6+134delinsCAGGGACCGCAG
ENST00000368567.4:c.6+123_6+134delinsCAGGGACCGCAG	ENSP00000357555.4:n.6+123_6+134delinsCAGGGACCGCAG
ENST00000392558.4:c.6+123_6+134delinsCAGGGACCGCAG	ENSP00000376341.4:n.6+123_6+134delinsCAGGGACCGCAG
ENST00000477151.1:n.52_63delinsCAGGGACCGCAG
ENST00000493224.5:n.163_174delinsCAGGGACCGCAG
NM_001030.4:c.6+123_6+134delinsCAGGGACCGCAG	NP_001021.1:n.6+123_6+134delinsCAGGGACCGCAG
NM_001030.6:c.6+123_6+134delinsCAGGGACCGCAG MANE Select	NP_001021.1:n.6+123_6+134delinsCAGGGACCGCAG
NM_001349946.1:c.-200_-189delinsCAGGGACCGCAG	NP_001336875.1:n.-200_-189delinsCAGGGACCGCAG
NM_001349947.1:c.-200_-189delinsCAGGGACCGCAG	NP_001336876.1:n.-200_-189delinsCAGGGACCGCAG
NM_001349946.2:c.-200_-189delinsCAGGGACCGCAG	NP_001336875.1:n.-200_-189delinsCAGGGACCGCAG
NM_001349947.2:c.-200_-189delinsCAGGGACCGCAG	NP_001336876.1:n.-200_-189delinsCAGGGACCGCAG